Allele Registry

Canonical Allele Identifier: PA113607

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019724

RCV000084570

RCV003509483

ClinVar Variation:

18097

HGVS (amino-acid)	Matching Registered Transcripts
NP_000475.1:p.Val715Met	CA127800 NM_000484.4:c.2143G>A